Search results for wnt4

83 hits were found for wnt4

# Family MCID Name MIFTS Score
1
MLL011 Mullerian Aplasia and Hyperandrogenism 46 19.816
2
46X054 46,xx Sex Reversal with Dysgenesis of Kidneys, Adrenals, and Lungs 26 5.355
3
P CLR023 Colorectal Cancer 99 4.057
4
HYP043 Hyperandrogenism 48 3.734
5
P HPT023 Hepatocellular Carcinoma 100 3.629
6
P END044 Endometriosis 63 3.324
7
AMN001 Amenorrhea 54 3.207
8
c 46X081 46,xx Sex Reversal 34 3.143
9
c BSL007 Basal Cell Carcinoma 68 2.566
10
P DSR089 Disorders of Sexual Development 45 2.566
11
HRM002 Hermaphroditism 36 2.566
12
MYR002 Mayer-Rokitansky-Kuster-Hauser Syndrome 58 2.109
13
P RNL100 Renal Hypodysplasia/aplasia 1 63 1.867
14
c 46X049 46,xy Sex Reversal 2 48 1.867
15
c 46X082 46,xy Sex Reversal 46 1.867
16
c PRM196 Premature Ovarian Failure 1 67 1.814
17
c WLM013 Wilms Tumor 1 65 1.814
18
NRR002 Norrie Disease 64 1.814
19
P EXD001 Exudative Vitreoretinopathy 55 1.814
20
ADR049 Adrenal Hypoplasia, Congenital 54 1.814
21
P PRS049 Persistent Mullerian Duct Syndrome 50 1.814
22
CKT002 Cakut 48 1.814
23
RNL025 Renal Hypoplasia 42 1.814
24
CHN064 Chondrodysplasia-Pseudohermaphroditism Syndrome 37 1.814
25
c 45X001 45,x/46,xy Mixed Gonadal Dysgenesis 33 1.814
26
SBM005 Submucous Uterine Fibroid 29 1.814
27
OVR009 Ovarian Gonadoblastoma 28 1.814
28
OVR057 Ovarian Serous Adenofibroma 27 1.814
29
OVR002 Ovarian Serous Cystadenofibroma 27 1.814
30
NNS042 Nonsyndromic Disorders of Testicular Development 21 1.814
31
AGN016 Aging 56 0.110
32
c NRF023 Neurofibromatosis, Type Ii 80 0.090
33
P THY023 Thymoma 65 0.090
34
FTT001 Fatty Liver Disease 61 0.090
35
P BND020 Bone Disease 59 0.090
36
THY029 Thyroid Carcinoma 59 0.090
37
ADN018 Adenoma 59 0.090
38
P INF032 Infertility 57 0.090
39
P PTT006 Pituitary Adenoma 55 0.090
40
c THY107 Thymoma, Familial 52 0.090
41
BNR002 Bone Resorption Disease 48 0.090
42
RNL077 Renal Fibrosis 47 0.090
43
URT010 Ureteral Obstruction 45 0.090
44
PTT037 Pituitary Tumors 44 0.090
45
P OVR042 Ovarian Cancer 88 0.064
46
c SYS001 Systemic Lupus Erythematosus 86 0.064
47
P GST053 Gastric Cancer 83 0.064
48
CRV035 Cervical Cancer 76 0.064
49
P OST002 Osteoporosis 74 0.064
50
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.064
51
P LYM118 Lymphoma 68 0.064
52
P LKM002 Leukemia 68 0.064
53
c ATS347 Autosomal Dominant Polycystic Kidney Disease 65 0.064
54
P PLY014 Polycystic Kidney Disease 62 0.064
55
LPP008 Lipoprotein Quantitative Trait Locus 62 0.064
56
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.064
57
P INT143 Interstitial Cystitis 61 0.064
58
HYD002 Hydronephrosis 60 0.064
59
ISC004 Ischemia 58 0.064
60
P BCL017 B-Cell Lymphoma 58 0.064
61
P FCL005 Focal Segmental Glomerulosclerosis 57 0.064
62
P MYS005 Myositis 56 0.064
63
P FBR017 Fibrosarcoma 56 0.064
64
P PLY011 Polycystic Ovary Syndrome 56 0.064
65
P MLN007 Male Infertility 55 0.064
66
P SCL048 Sclerosteosis 55 0.064
67
SCH038 Schopf-Schulz-Passarge Syndrome 55 0.064
68
P OVR049 Ovarian Disease 52 0.064
69
P MMB011 Membranous Nephropathy 50 0.064
70
PLP001 Pulpitis 49 0.064
71
ATS010 Autosomal Recessive Disease 48 0.064
72
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.064
73
HYP068 Hyperostosis 48 0.064
74
IGG001 Iga Glomerulonephritis 48 0.064
75
DWR001 Dwarfism 44 0.064
76
P SPN081 Spondylocostal Dysostosis, Autosomal Recessive 43 0.064
77
HYP457 Hypertrophic Scars 42 0.064
78
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.064
79
MYS001 Myositis Ossificans 41 0.064
80
OVR094 Ovarian Epithelial Cancer 38 0.064
81
GLM044 Glomerular Disease 37 0.064
82
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.064
83
UTR054 Uterine Hypoplasia 25 0.064
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